Intravenous Ibuprofen Reduces Opioid Consumption During the Initial 48 Hours After Injury in Orthopedic Trauma Patients.


Journal

Journal of orthopaedic trauma
ISSN: 1531-2291
Titre abrégé: J Orthop Trauma
Pays: United States
ID NLM: 8807705

Informations de publication

Date de publication:
Jul 2020
Historique:
pubmed: 14 1 2020
medline: 22 6 2021
entrez: 14 1 2020
Statut: ppublish

Résumé

To evaluate the efficacy of intravenous (IV) ibuprofen (Caldolor) administration in the management of acute pain in orthopedic trauma patients and to minimize opioid use. Randomized controlled trial, double-blind, parallel, placebo-controlled. Level 1 Trauma Center. A total of 99 consecutive orthopedic trauma patients with fractures of the ribs, face, extremities, and/or pelvis were randomized to receive either 800 mg IV ibuprofen (53 patients) or placebo (44 patients) administered every 6 hours for a total of 8 doses within 48 hours of admission and the same PRN medications along with 20-mg IV/PO Pepcid twice a day. To establish pain reduction efficacy, the analysis was consequently performed in the modified intent-to-treat group that included 74 randomized subjects with a baseline pain score greater than 2. The primary outcomes were reduction in opioid consumption and decrease in pain intensity (PI). Administration of study medications. PI measured by Numerical Rating Scale, opioid consumption adjusted to morphine equivalent dose, and time to first narcotic administration. The 2 groups had comparable baseline characteristics: age, sex distribution, mechanism of injury, type of injury, injury severity score, and PI. IV ibuprofen statistically significantly reduced opioid consumption compared with placebo during the initial 48-hour period (P = 0.017). PI calculated as PI differences was statistically different only at 8-hour interval after Caldolor administration. Time to first narcotic medication was significantly longer in the Caldolor group (hazard ratio: 1.640; 95% confidence interval, 1.009-2.665; P = 0.046). IV ibuprofen provided adequate analgesia, prolonged time to first narcotic administration, and was opioid-sparing for the treatment of pain in orthopedic trauma patients, which makes Caldolor a recommended candidate for managing acute pain in the diverse orthopaedic trauma population. Therapeutic Level I. See Instructions for Authors for a complete description of levels of evidence.

Identifiants

pubmed: 31929374
doi: 10.1097/BOT.0000000000001733
pmc: PMC7274153
pii: 00005131-202007000-00002
doi:

Substances chimiques

Analgesics, Non-Narcotic 0
Analgesics, Opioid 0
Ibuprofen WK2XYI10QM

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

341-347

Références

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Auteurs

Russell D Weisz (RD)

Delray Medical Center, Delray Beach, FL.

Alexander A Fokin (AA)

Delray Medical Center, Delray Beach, FL.

Vivian Lerner (V)

Delray Medical Center, Delray Beach, FL.

Amy Flynt (A)

PharPoint Research, Durham, NC; and.

Ines Macias-Perez (I)

Cumberland Pharmaceuticals, Nashville, TN.

Leo Pavliv (L)

Cumberland Pharmaceuticals, Nashville, TN.

Maggie Crawford (M)

Delray Medical Center, Delray Beach, FL.

Ivan Puente (I)

Delray Medical Center, Delray Beach, FL.

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Classifications MeSH